Recombinant ERG Monoclonal Antibody (AN301715L)

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For research use only.
Verified Samples |
Verified Samples in WB: Jurkat Verified Samples in IHC: Human kidney, Human prostate cancer, Mouse cerebrum, Rat kidney Verified Samples in IF: THP-1 Verified Samples in FCM: THP-1 |
Dilution | WB 1:500-1:2000, IHC 1:100-1:1000, IF 1:50-1:100, FCM 1:50-1:100 |
Isotype | IgG, κ |
Host | Rabbit |
Reactivity | Human, Rat, Mouse |
Applications | WB, IHC, IF, FCM |
Clonality | Monoclonal;Recombinant |
Immunogen | Recombinant human ERG fragment |
Abbre | ERG |
Synonyms | ERG, Avian erythroblastosis virus E-26 (v-ets) oncogene related, D030036I24Rik, Erg 3, ERG/EWS fusion gene, ERG/FUS fusion gene, ERG/TMPSSR2 fusion gene, ERG1, ERG2, ets related, ETS-related gene, included, isoform CRA_e, KCNH2, Oncogene ERG, p55, TMPRSS2/ERG fusion, Transcriptional regulator ERG, transcriptional regulator ERG (transforming protein ERG), Transforming protein ERG, v ets avian erythroblastosis virus E26 oncogene, v ets avian erythroblastosis virus E26 oncogene related, v ets erythroblastosis virus E26 oncogene homolog, v ets erythroblastosis virus E26 oncogene like, v ets erythroblastosis virus E26 oncogene like isoform 2, v-ets erythroblastosis virus E26 oncogene, v-ets erythroblastosis virus E26 oncogene homolog (avian), V-ets erythroblastosis virus E26 oncogene like (Avian) |
Swissprot | |
Calculated MW | 54 kDa |
Observed MW |
54 kDa
Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include: 1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein. 2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes. 3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1. 4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids). 5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers. If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane. |
Cellular Localization | Cytoplasm, Nucleus |
Concentration | 1 mg/mL |
Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
Purification Method | Protein A purified |
Research Areas | Epigenetics and Nuclear Signaling, Stem Cells |
Clone No. | A423 |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | Ice bag |
background | ERG is a transcriptional regulator. It may participate in transcriptional regulation through the recruitment of SETDB1 histone methyltransferase and subsequent modification of local chromatin structure. |
Other Clones
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Other Formats
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Unconjugated
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